Canonical Allele Identifier: CA1803281025

Gene: PDP1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.93923641_93923643delinsCAT , CM000670.2:g.93923641_93923643delinsCAT	GRCh38
NC_000008.10:g.94935869_94935871delinsCAT , CM000670.1:g.94935869_94935871delinsCAT	GRCh37
NC_000008.9:g.95005045_95005047delinsCAT	NCBI36
NG_012233.1:g.11708_11710delinsCAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297598.5:c.1582_1584delinsCAT MANE Select	ENSP00000297598.4:p.His528=
ENST00000297598.4:c.1582_1584delinsCAT	ENSP00000297598.4:p.His528=
ENST00000396200.3:c.1657_1659delinsCAT	ENSP00000379503.3:p.His553=
ENST00000517764.1:c.1582_1584delinsCAT	ENSP00000430380.1:p.His528=
ENST00000520728.5:c.1582_1584delinsCAT	ENSP00000428317.1:p.His528=
NM_001161779.1:c.1657_1659delinsCAT	NP_001155251.1:p.His553=
NM_001161780.1:c.1657_1659delinsCAT	NP_001155252.1:p.His553=
NM_001161781.1:c.1582_1584delinsCAT	NP_001155253.1:p.His528=
NM_018444.3:c.1582_1584delinsCAT	NP_060914.2:p.His528=
XM_011517135.1:c.1636_1638delinsCAT	XP_011515437.1:p.His546=
XM_011517136.1:c.1582_1584delinsCAT	XP_011515438.1:p.His528=
XM_011517137.1:c.1582_1584delinsCAT	XP_011515439.1:p.His528=
XM_011517135.2:c.1636_1638delinsCAT	XP_011515437.1:p.His546=
XM_011517136.2:c.1582_1584delinsCAT	XP_011515438.1:p.His528=
XM_017013588.1:c.1744_1746delinsCAT	XP_016869077.1:p.His582=
NM_018444.4:c.1582_1584delinsCAT MANE Select	NP_060914.2:p.His528=
NM_001161780.2:c.1657_1659delinsCAT	NP_001155252.1:p.His553=
NM_001161781.2:c.1582_1584delinsCAT	NP_001155253.1:p.His528=
NM_001161779.2:c.1657_1659delinsCAT	NP_001155251.1:p.His553=